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新型紫杉醇-氯法齐明纳米颗粒共制剂的抗癌疗效及毒代动力学

Anticancer efficacy and toxicokinetics of a novel paclitaxel-clofazimine nanoparticulate co-formulation.

作者信息

Koot Dwayne, Cromarty Duncan

机构信息

Department of Pharmacology, Faculty of Health Sciences, University of Pretoria, PO Box 2034, Pretoria, 0001, South Africa,

出版信息

Drug Deliv Transl Res. 2015 Jun;5(3):257-67. doi: 10.1007/s13346-015-0222-6.

Abstract

Contemporary chemotherapy is limited by disseminated, resistant cancer. Targeting nanoparticulate drug delivery systems that encapsulate synergistic drug combinations are a rational means to increase the therapeutic index of chemotherapeutics. A lipopolymeric micelle co-encapsulating an in vitro optimized, synergistic fixed-ratio combination of paclitaxel (PTX) and clofazimine (B663) has been developed and called Riminocelles™. The present pre-clinical study investigated the acute toxicity, systemic exposure, repeat dose toxicity and efficacy of Riminocelles in parallel to Taxol® at an equivalent PTX dose of 10 mg/kg. Daily and weekly dosing schedules were evaluated against Pgp-expressing human colon adenocarcinoma (HCT-15) xenografts implanted subcutaneously in athymic mice. Riminocelles produced statistically significant (p <  .05) tumor growth delays of 3.2 and 2.7 days for the respective schedules in contrast to Taxol delaying growth by 0.5 and 0.6 days. Using the control tumor doubling time of 4.2 days, tumor-cell-kill values of 0.23 for Riminocelles and 0.04 for Taxol following daily schedules were calculated. A significant weight loss of 5.7% after 14 days (p < 0.05) relative to the control group (n = 8) was observed for the daily Taxol group whereas Riminocelles did not incur significant weight loss neither were blood markers of toxicity elevated after acute administration (n = 3). The safety and efficacy of Riminocelles is statistically superior to Taxol. However, passive tumor targeting was not achieved and the tumor burden progressed quickly. Prior to further animal studies, the in vivo thermodynamic instability of the simple lipopolymeric micellular delivery system requires improvement so as to maintain and selectively deliver the fixed-ratio drug combination.

摘要

当代化疗受到播散性耐药癌症的限制。靶向包裹协同药物组合的纳米颗粒药物递送系统是提高化疗药物治疗指数的合理手段。已开发出一种共包裹体外优化的紫杉醇(PTX)和氯法齐明(B663)协同固定比例组合的脂质聚合物胶束,并将其命名为Riminocelles™。本临床前研究在等效PTX剂量为10mg/kg的情况下,与紫杉醇®平行研究了Riminocelles的急性毒性、全身暴露、重复剂量毒性和疗效。针对植入无胸腺小鼠皮下的表达Pgp的人结肠腺癌(HCT-15)异种移植物,评估了每日和每周给药方案。与紫杉醇分别使肿瘤生长延迟0.5天和0.6天相比,Riminocelles在各自给药方案下使肿瘤生长延迟3.2天和2.7天,具有统计学显著性(p<0.05)。使用对照肿瘤倍增时间4.2天,计算出每日给药方案后Riminocelles的肿瘤细胞杀伤值为0.23,紫杉醇为0.04。每日紫杉醇组在14天后相对于对照组(n = 8)体重显著减轻5.7%(p < 0.05),而Riminocelles未导致显著体重减轻,急性给药后毒性血液标志物也未升高(n = 3)。Riminocelles的安全性和疗效在统计学上优于紫杉醇。然而,未实现被动肿瘤靶向,肿瘤负荷进展迅速。在进一步的动物研究之前,简单脂质聚合物胶束递送系统的体内热力学不稳定性需要改善,以维持并选择性递送固定比例的药物组合。

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